Alba, Liliana
Loading...
1
0
20
0
false
Nombre completo
Alba, Liliana
Publicaciones
(Articles)
Results 1-7 of 7 (Search time: 0.039 seconds).
| Issue Date | Title | Author(s) | |
|---|---|---|---|
| 1 | Oct-2004 | Acitretin embryopathy: a case report | Barbero, Pablo ; Lotersztein, Vanesa ; Bronberg, Rubén ; Perez, Miriam ; Alba, Liliana |
| 2 | Feb-2006 | Censo de servicios de genética médica en Argentina | Liascovich, Rosa ; Rozental, Sandra ; Barbero, Pablo ; Alba, Liliana ; Ortiz, Zulma |
| 3 | 15-Jul-2013 | Isolated p.H62L Mutation in the CYP21A2 Gene in a Simple Virilizing 21-Hydroxylase Deficient Patient | Taboas, Melisa ; Fernandez, Cecilia ; Belli, Susana ; Buzzalino, Noemí ; Alba, Liliana ; Dain, Liliana |
| 4 | Mar-1996 | Microcephaly, characteristic facies, joint abnormalities, and deficient leucocyte chemotaxis: a further case of the syndrome of Say et al | Perandones, Claudia ; Cerretini, Roxana Inés ; Vargas Vera, R M ; Aranda, Eliseo Isaac ; Alba, Liliana ; Pivetta, Omar H. |
| 5 | Jun-2008 | Síndrome de insensibilidad completa a los andrógenos : diagnóstico y características clínicas | Solari, Andrea ; Groisman, Boris ; Bidondo, María P. ; Cinca, Constanza ; Alba, Liliana |
| 6 | Dec-2016 | Structure-based activity prediction of CYP21A2 stability variants: A survey of available gene variations | Bruque, Carlos David ; Delea, Marisol ; Fernández, Cecilia ; Orza, Juan V ; Taboas, Melisa ; Buzzalino, Noemí ; Espeche, Lucía ; Solari, Andrea ; Luccerini, Verónica ; Alba, Liliana ; Nadra, Alejandro D. ; Dain, Liliana |
| 7 | 2011 | Structure-based analysis of five novel disease-causing mutations in 21-hydroxylase-deficient patients | Minutolo, Carolina ; Nadra, Alejandro D. ; Fernández, Cecilia ; Taboas, Melisa ; Buzzalino, Noemí ; Casali, Bárbara ; Belli, Susana ; Charreau, Eduardo H. ; Alba, Liliana ; Dain, Liliana |